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仙台副粘病毒6/94在C129小鼠中的终身持续存在:通过与克隆的基因组cDNA探针杂交检测潜伏病毒RNA

Lifelong persistence of paramyxovirus Sendai-6/94 in C129 mice: detection of a latent viral RNA by hybridization with a cloned genomic cDNA probe.

作者信息

Koch E M, Neubert W J, Hofschneider P H

出版信息

Virology. 1984 Jul 15;136(1):78-88. doi: 10.1016/0042-6822(84)90249-6.

Abstract

C129 mice infected intracerebrally with Sendai-6/94 virus were examined periodically for the presence of viral proteins and viral RNA over a span of 423 days. On postinfection Day 15 (PID 15) an acute infection was demonstrated by increased anti-6/94 antibody titers and expression of viral proteins. More than a year later, on PIDs 373 and 423, no viral antigens were detected. Rescue of infectious virus from the mouse brains was only observable for 74 days following cocultivation of the cells on PID 15. Later, no signs of viral persistence were found at the protein level. In a further experiment, the murine tissues and cell cultures were examined for the presence of viral RNA. Virus-specific cDNA was cloned in the bacteriophage lambda system and used as a highly specific hybridization probe. Surprisingly, 6/94 viral RNA was detectable lifelong in the brain tissue of infected mice although no proteins were expressed. Murine brain cells cocultivated on PID 15 still contained viral RNA after 245 days in culture, although the expression of viral proteins was measureable for only 80 days. The results indicate a stable latency of the 6/94 virus in cell cultures and in animals at the RNA level without detectable protein expression.

摘要

对经脑内接种仙台-6/94病毒感染的C129小鼠,在423天的时间跨度内定期检测病毒蛋白和病毒RNA的存在情况。在感染后第15天(PID 15),抗6/94抗体滴度升高和病毒蛋白表达表明存在急性感染。一年多后,在PID 373和423时,未检测到病毒抗原。仅在PID 15将细胞共培养后74天内可观察到从小鼠脑中拯救出感染性病毒。后来,在蛋白质水平未发现病毒持续存在的迹象。在进一步的实验中,检测了鼠组织和细胞培养物中病毒RNA的存在情况。病毒特异性cDNA克隆到噬菌体λ系统中,并用作高度特异性的杂交探针。令人惊讶的是,尽管未表达蛋白质,但在感染小鼠的脑组织中可终身检测到6/94病毒RNA。在PID 15共培养的鼠脑细胞在培养245天后仍含有病毒RNA,尽管病毒蛋白的表达仅在80天内可检测到。结果表明,6/94病毒在细胞培养物和动物中在RNA水平存在稳定的潜伏期,且未检测到蛋白质表达。

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